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Ring fragmentation processes resulting from acid catalysed diazo ketone cyclisations
Authors:Oliver E Hutt  Anthony C Willis
Institution:Research School of Chemistry, Australian National University, Canberra, ACT 0200, Australia
Abstract:The initial products from the cyclisation of hexahydrophenanthryl diazo ketones with participation by either the alkene bonds or the aromatic ring (Ar1,4) undergo rearrangement by 1,2 bond shifts or unexpected bond fission. Benzocyclo-octanyl ketones were formed from the latter process.
Keywords:Diazo ketone  Cyclisation  Ring fragmentation  Benzocyclo-octanones
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